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United States · US · US:85766-041_4e91823d-9f37-5437-e063-6294a90a0cd0
CYCLOBENZAPRINE HYDROCHLORIDE
Orange BookUNIISPLATC M03BX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSportpharm LLC
CountryUS (United States)
ATC codeM03BX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 16
- ndc1185766041001000 TABLET, FILM COATED in 1 BOTTLE (85766-041-00)
- ndc1185766041011 TABLET, FILM COATED in 1 BOTTLE (85766-041-01)
- ndc1185766041022 TABLET, FILM COATED in 1 BOTTLE (85766-041-02)
- ndc1185766041033 TABLET, FILM COATED in 1 BOTTLE (85766-041-03)
- ndc1185766041044 TABLET, FILM COATED in 1 BOTTLE (85766-041-04)
- ndc1185766041055 TABLET, FILM COATED in 1 BOTTLE (85766-041-05)
- ndc1185766041077 TABLET, FILM COATED in 1 BOTTLE (85766-041-07)
- ndc11857660410910 TABLET, FILM COATED in 1 BOTTLE (85766-041-09)
- ndc118576604110100 TABLET, FILM COATED in 1 BOTTLE (85766-041-10)
- ndc11857660411414 TABLET, FILM COATED in 1 BOTTLE (85766-041-14)
- ndc11857660411515 TABLET, FILM COATED in 1 BOTTLE (85766-041-15)
- ndc11857660412020 TABLET, FILM COATED in 1 BOTTLE (85766-041-20)
- ndc11857660413030 TABLET, FILM COATED in 1 BOTTLE (85766-041-30)
- ndc118576604150500 TABLET, FILM COATED in 1 BOTTLE (85766-041-50)
- ndc11857660416060 TABLET, FILM COATED in 1 BOTTLE (85766-041-60)
- ndc11857660419090 TABLET, FILM COATED in 1 BOTTLE (85766-041-90)
Annotations
UNII (FDA Substance ID)
0VE05JYS2P
CYCLOBENZAPRINE HYDROCHLORIDE
RxCUI 52101
Orange Book
A208170
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0VE05JYS2P",
"rxcui": "52101",
"inchikey": "VXEAYBOGHINOKW-UHFFFAOYSA-N",
"display_name": "CYCLOBENZAPRINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"fe81c68d-a579-4fe9-e053-6294a90a7bc0": {
"match": "brand_token",
"title": "CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY]",
"spl_version": "8",
"published_date": "2026-06-01"
}
},
"productid": "85766-041_4e91823d-9f37-5437-e063-6294a90a0cd0",
"productndc": "85766-041",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "208170",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "May 31, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "7.5MG",
"product_no": "002",
"approval_date": "May 31, 2017"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "003",
"approval_date": "May 31, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CYCLOBENZAPRINE HYDROCHLORIDE",
"proprietary_name": "CYCLOBENZAPRINE HYDROCHLORIDE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA208170",
"marketing_category": "ANDA",
"nonproprietary_name": "cyclobenzaprine hydrochloride",
"start_marketing_date": "20170531",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code M03BX08.
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